Inherited mitochondrial DNA depletion

被引:23
作者
Elpeleg, O [1 ]
机构
[1] Shaare Zedek Med Ctr, Metab Dis Unit, IL-91031 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Fac Med, IL-91031 Jerusalem, Israel
关键词
D O I
10.1203/01.PDR.0000072796.25097.A5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Mitochondrial DNA (mtDNA) depletion is associated with heterogeneous clinical phenotypes. The recent identification of the mutated genes in three groups of patients with mtDNA depletion had underscored the importance of the synthetic pathway of the mitochondrial nucleotides for mtDNA replication. Future goals include understanding how the defective proteins perturb replication, why it affects only some tissues and spares others, and which other genes should be considered in other patients with mtDNA depletion.
引用
收藏
页码:153 / 159
页数:7
相关论文
共 62 条
  • [1] DEPLETION OF MUSCLE MITOCHONDRIAL-DNA IN AIDS PATIENTS WITH ZIDOVUDINE-INDUCED MYOPATHY
    ARNAUDO, E
    DALAKAS, M
    SHANSKE, S
    MORAES, CT
    DIMAURO, S
    SCHON, EA
    [J]. LANCET, 1991, 337 (8740) : 508 - 510
  • [2] MAMMALIAN DEOXYRIBONUCLEOSIDE KINASES
    ARNER, ESJ
    ERIKSSON, S
    [J]. PHARMACOLOGY & THERAPEUTICS, 1995, 67 (02) : 155 - 186
  • [3] Late-onset mitochondrial DNA depletion:: DNA copy number, multiple deletions, and compensation
    Barthélémy, C
    de Baulny, HO
    Diaz, J
    Cheval, MA
    Frachon, P
    Romero, N
    Goutieres, F
    Fardeau, M
    Lombès, A
    [J]. ANNALS OF NEUROLOGY, 2001, 49 (05) : 607 - 617
  • [4] BESTWICK RK, 1982, J BIOL CHEM, V257, P9305
  • [5] Cell cycle-dependent metabolism of pyrimidine deoxynucleoside triphosphates in CEM cells
    Bianchi, V
    Borella, S
    Rampazzo, C
    Ferraro, P
    Calderazzo, F
    Bianchi, LC
    Skog, S
    Reichard, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (26) : 16118 - 16124
  • [6] Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures
    Blake, JC
    Taanman, JW
    Morris, AMM
    Gray, RGF
    Cooper, JM
    McKiernan, PJ
    Leonard, JV
    Schapira, AHV
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (01) : 67 - 70
  • [7] BODNAR AG, 1993, AM J HUM GENET, V53, P663
  • [8] BOGENHAGEN D, 1976, J BIOL CHEM, V251, P2938
  • [9] MITOCHONDRIAL CYTOCHROME DEFICIENCY PRESENTING AS A MYOPATHY WITH HYPOTONIA, EXTERNAL OPHTHALMOPLEGIA, AND LACTIC-ACIDOSIS IN AN INFANT AND AS FATAL HEPATOPATHY IN A 2ND COUSIN
    BOUSTANY, RN
    APRILLE, JR
    HALPERIN, J
    LEVY, H
    DELONG, GR
    [J]. ANNALS OF NEUROLOGY, 1983, 14 (04) : 462 - 470
  • [10] DEATHS IN US FIALURIDINE TRIAL
    BRAHAMS, D
    [J]. LANCET, 1994, 343 (8911) : 1494 - 1495